MedPath

Thrombin Generation and Gestational Outcome

Completed
Conditions
Thrombophilia
Registration Number
NCT02139670
Lead Sponsor
HaEmek Medical Center, Israel
Brief Summary

In total 120 pregnant women's with history of recurrent miscarriages, are planned for inclusion in this trial. After signing an informed consent a blood sample will be obtained from each participant. The investigators will measure the thrombin generation in plasma assessed by the calibrated automated thrombogram (CAT). The relation between pregnancy outcome and thrombin measurements will be determined

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
29
Inclusion Criteria
  • age > 18
  • signed inform consent
  • first trimester
  • two early miscarriages(before week 10) or one later abortions (after week 10)
Exclusion Criteria
  • Chronic treatment with aspirin or other anticoagulants

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
pregnancy outcome2 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Haemek medical center

🇮🇱

Afula, Israel

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